Canonical Allele Identifier: CA2244610965

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899540C= , CM000679.2:g.4899540C=	GRCh38
NC_000017.10:g.4802835C= , CM000679.1:g.4802835C=	GRCh37
NC_000017.9:g.4743614C=	NCBI36
NG_008029.2:g.8536G=
NG_028005.1:g.71201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.-223C= (C17orf107) MANE Select	ENSP00000370770.3:n.-223C=
ENST00000649488.2:c.960G= (CHRNE) MANE Select	ENSP00000497829.1:p.Met320=
ENST00000649830.1:c.27G= (CHRNE)	ENSP00000496907.1:p.Met9=
ENST00000652550.1:n.690G= (CHRNE)
ENST00000293780.4:c.960G= (CHRNE)	ENSP00000293780.4:p.Met320=
ENST00000381365.3:c.-223C= (C17orf107)	ENSP00000370770.3:n.-223C=
ENST00000521575.1:c.-223C= (C17orf107)	ENSP00000429241.1:n.-223C=
ENST00000572438.1:n.646G= (CHRNE)
NM_000080.3:c.960G= (CHRNE)	NP_000071.1:p.Met320=
XM_011523612.1:c.-223C= (C17orf107)	XP_011521914.1:n.-223C=
XM_011523631.1:c.845G= (CHRNE)	XP_011521933.1:p.Ter282=
NM_000080.4:c.960G= (CHRNE) MANE Select	NP_000071.1:p.Met320=
XM_017024115.1:c.924G= (CHRNE)	XP_016879604.1:p.Met308=
XR_001752421.1:n.1690G= (CHRNE)
NM_001145536.2:c.-223C= (C17orf107) MANE Select	NP_001139008.1:n.-223C=